510(k) K171329 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Altus Spine Titanium Interbody Fusion System
| Applicant | Altus Partners, LLC, West Chester PA, US |
| Decision | Substantially Equivalent, Aug 29, 2017 |
| Received | May 5, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K171329
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.